Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/- | Ancestral: C | MAF: 0.45 (-)
Location

Chromosome 11:102799765 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 4 HGVS names - click the plus to show

11:g.102799765delC
ENST00000525739.4:n.682+1644delC
ENST00000371455.5:n.423+1644delC
ENST00000544704.1:n.443+1644delC

Variation displays